Schedule for Rating Disabilities: The Hematologic and Lymphatic Systems. Final rule [0.03%]
关于残疾补偿的评定时间表：血液和淋巴系统。最终规则
Department of Veterans Affairs
Department of Veterans Affairs
This document amends the Department of Veterans Affairs (VA) Schedule for Rating Disabilities (VASRD) by revising the section of the Rating Schedule that addresses the hematologic and lymphatic systems. This action will ensure VA uses curre...
Medical Devices; Ear, Nose, and Throat Devices; Classification of the Active Implantable Bone Conduction Hearing System. Final order [0.03%]
医疗器械；耳鼻喉器械；主动植入式骨导听觉系统装置的分类决定终局命令公告
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the active implantable bone conduction hearing system into class II (special controls). The special controls that apply to the device type are identified in this order and will be ...
Medical Devices; Anesthesiology Devices; Classification of the High Flow Humidified Oxygen Delivery Device. Final order [0.03%]
医疗器械；麻醉机和呼吸设备；关于高流量加温湿化氧疗装置的分类决定（最终令）
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the high flow humidified oxygen delivery device into class II (special controls). The special controls that apply to the device type are identified in this order and will be part o...
Presumption of Herbicide Exposure and Presumption of Disability During Service for Reservists Presumed Exposed to Herbicides. Final rule [0.03%]
关于认定 reservist 的除草剂接触情况以及认定接触除草剂的 reservist 在服役期间出现残疾的情况的规定（最终规则）
Department of Veterans Affairs
Department of Veterans Affairs
The Department of Veterans Affairs (VA) is adopting as final an interim final rule published on June 19, 2015, to amend its adjudication regulation governing individuals presumed to have been exposed to certain herbicides. Specifically, VA ...
Medical Devices; Ophthalmic Devices; Classification of the Intranasal Electrostimulation Device for Dry Eye Symptoms. Final order [0.03%]
医疗器械；眼科学设备；干眼症鼻内电刺激装置的分类。最终命令
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the intranasal electrostimulation device for dry eye symptoms into class II (special controls). The special controls that apply to the device type are identified in this order and ...
Medical Devices; Neurological Devices; Classification of the Thermal Vestibular Stimulator for Headache. Final order [0.03%]
医疗器械；神经病学器械；头痛热前庭刺激仪分类决定终稿
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the thermal vestibular stimulator for headache into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of...
Medical Devices; General and Plastic Surgery Devices; Classification of the Hemostatic Device for Intraluminal Gastrointestinal Use. Final order [0.03%]
医疗器械；一般和整形外科器械；内窥镜用止血设备分类决定（最终版）
Food and Drug Administration, HHS.
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the hemostatic device for intraluminal gastrointestinal use into class II (special controls). The special controls that apply to the device type are identified in this order and wi...
Medical Devices; General and Plastic Surgery Devices; Classification of the Light Based Energy Source Device for Topical Application. Final order [0.03%]
医疗器械；一般和整形外科器械；用于体表应用的基于光线能量源设备的分类。最终命令
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the light based energy source device for topical application into class II (special controls). The special controls that apply to the device type are identified in this order and w...
Medical Devices; General and Plastic Surgery Devices; Classification of the Wound Autofluorescence Imaging Device. Final order [0.03%]
医疗器械；一般和整形外科器械；伤口自体荧光成像设备的分类决定（最终版）
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the wound autofluorescence imaging device into class I. We are taking this action because we have determined that classifying the device into class I will provide a reasonable assu...
Medical Devices; Anesthesiology Devices; Classification of the Positive Airway Pressure Delivery System. Final order [0.03%]
医疗器械；麻醉机和呼吸设备；关于持续气道正压递送系统的分类决定（定稿）
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the positive airway pressure delivery system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of t...